TY - JOUR
T1 - Y-box binding protein-1 is a novel molecular target for tumor vessels
AU - Takahashi, Mayu
AU - Shimajiri, Shohei
AU - Izumi, Hiroto
AU - Hirano, Gen
AU - Kashiwagi, Eiji
AU - Yasuniwa, Yoshihiro
AU - Wu, Ying
AU - Han, Bin
AU - Akiyama, Masaki
AU - Nishizawa, Shigeru
AU - Sasaguri, Yasuyuki
AU - Kohno, Kimitoshi
PY - 2010/6
Y1 - 2010/6
N2 - Y-box binding protein-1 (YB-1) is a member of the cold shock protein family and functions in transcription and translation. Many reports indicate that YB-1 is highly expressed in tumor cells and is a marker for tumor aggressiveness and clinical prognosis. Here, we show clear evidence that YB-1 is expressed in the angiogenic endothelial cells of various tumors, such as glioblastoma, esophageal cancer, gastric cancer, colon cancer, and lung cancer, as well as in tumor cells. YB-1 was highly expressed in glomeruloid microvascular endothelial cells of brain tumors and microvessels in the desmoplastic region around multiple solid tumors. On the other hand, no or low YB-1 expression was observed in normal angiogenic endothelial cells from fetal kidney, newborn lung, and placenta. The endothelial cells in inflammatory regions of granulomas were also weakly labeled. Knockdown of YB-1 expression by small-interfering RNA induced G1 cell cycle arrest and inhibited the growth of human umbilical vein endothelial cells stimulated by growth factors. Taken together, YB-1 plays an important role in the growth of not only tumor cells but also tumor-associated endothelial cells, suggesting that YB-1 is a promising target for cancer therapy. Cancer Sci 2010).
AB - Y-box binding protein-1 (YB-1) is a member of the cold shock protein family and functions in transcription and translation. Many reports indicate that YB-1 is highly expressed in tumor cells and is a marker for tumor aggressiveness and clinical prognosis. Here, we show clear evidence that YB-1 is expressed in the angiogenic endothelial cells of various tumors, such as glioblastoma, esophageal cancer, gastric cancer, colon cancer, and lung cancer, as well as in tumor cells. YB-1 was highly expressed in glomeruloid microvascular endothelial cells of brain tumors and microvessels in the desmoplastic region around multiple solid tumors. On the other hand, no or low YB-1 expression was observed in normal angiogenic endothelial cells from fetal kidney, newborn lung, and placenta. The endothelial cells in inflammatory regions of granulomas were also weakly labeled. Knockdown of YB-1 expression by small-interfering RNA induced G1 cell cycle arrest and inhibited the growth of human umbilical vein endothelial cells stimulated by growth factors. Taken together, YB-1 plays an important role in the growth of not only tumor cells but also tumor-associated endothelial cells, suggesting that YB-1 is a promising target for cancer therapy. Cancer Sci 2010).
UR - http://www.scopus.com/inward/record.url?scp=77954156987&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77954156987&partnerID=8YFLogxK
U2 - 10.1111/j.1349-7006.2010.01534.x
DO - 10.1111/j.1349-7006.2010.01534.x
M3 - Article
C2 - 20398058
AN - SCOPUS:77954156987
SN - 1347-9032
VL - 101
SP - 1367
EP - 1373
JO - Cancer Science
JF - Cancer Science
IS - 6
ER -